ARHGEF33

mutation — cross-omics
Cross-omicsMUTATION → RNACell-linePairwise association · TCGA cohorts

Across TCGA cell cohorts, ARHGEF33 mutation is significantly associated with the RNA expression of many other genes, with 169 significant associations in total. LARGE_INTESTINE shows the largest number of these associations.

The most reproducible ARHGEF33-associated genes across cancer lineages are ACSM2A, OR13C9, and RSPH6A. Each is linked with ARHGEF33 in more than 1 cancer types. Because this analysis shows association rather than direction, both ARHGEF33-to-partner and partner-to-ARHGEF33 results are reported.

Each partner links to its own Q-omics profile.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (ARHGEF33→partner) and Y-score (partner→ARHGEF33) are standardized regression coefficients; both directions are reported because the association is undirected. p-values are from the association test.
LineagePartner geneX-scoreY-scorep(X)p(Y)Sampling consensusLineage consensus
OVARYACSM2A →+0.047+4.029.003.00932
OVARYOR13C9 →+0.041+4.228<.001.00631
CNSRSPH6A →+0.033+3.874<.001.00631
CNSZNF831 →+0.070+3.832<.001.00531
CNSIL22RA2 →+0.425+4.584<.001.00131
CNSOR6C2 →+0.095+4.044<.001.00331
Each partner links to its Q-omics profile. Showing the 6 strongest of 169 associations by consensus.

Exploration